Evidence map›Paper›PMID 42444331›Full record

ArticleAnalytical chemistry2026

Forensic Electrochemistry: A Dual-Mode Strategy for Rapid and Selective Detection of Catecholamine Compounds.

Larissa M A Melo, Elena Bernalte, Robert D Crapnell, Rodrigo M Verly, Rodrigo A A Muñoz, Wallans T P Dos Santos, Craig E Banks

Abstract read
In one paragraph

Article in Analytical chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Larissa M A MeloFaculty of Science and Engineering, Dalton Building, Manchester Metropolitan University, Chester Street, ManchesterM1 5GD, United Kingdom.
Elena BernalteFaculty of Science and Engineering, Dalton Building, Manchester Metropolitan University, Chester Street, ManchesterM1 5GD, United Kingdom.ORCID 0000-0002-0764-789X
Robert D CrapnellFaculty of Science and Engineering, Dalton Building, Manchester Metropolitan University, Chester Street, ManchesterM1 5GD, United Kingdom.ORCID 0000-0002-8701-3933
Rodrigo M VerlyDepartment of Chemistry, Federal University of Vales do Jequitinhonha and Mucuri, Campus JK, Diamantina, Minas Gerais39100000, Brazil.
Rodrigo A A MuñozInstitute of Chemistry, Federal University of Uberlândia, Uberlândia, Minas Gerais38400-902, Brazil.ORCID 0000-0001-8230-5825
Wallans T P Dos SantosDepartment of Pharmacy, Federal University of Vales do Jequitinhonha and Mucuri, Campus JK, Diamantina, Minas Gerais39100000, Brazil.ORCID 0000-0001-6585-9930
Craig E BanksFaculty of Science and Engineering, Dalton Building, Manchester Metropolitan University, Chester Street, ManchesterM1 5GD, United Kingdom.ORCID 0000-0002-0756-9764

Funding

Conselho Nacional de Desenvolvimento Cient??fico e Tecnol??gico 308152/2025-5Conselho Nacional de Desenvolvimento Cient??fico e Tecnol??gico 315838/2021-3Conselho Nacional de Desenvolvimento Cient??fico e Tecnol??gico 406309/2025-6Coordena????o de Aperfei??oamento de Pessoal de N??vel Superior Finance Code 001Funda????o de Amparo ls Pesquisa do Estado de Minas Gerais APQ-01996-23Funda????o de Amparo ls Pesquisa do Estado de Minas Gerais APQ-04955-23Funda????o de Amparo ls Pesquisa do Estado de Minas Gerais RED-00120-23INCT-SP 406958/2022-0INCT-SP APQ-03984-24INCT-SP NA
6 · The paper itself

Abstract

A novel colorimetric-electrochemical strategy was developed for the selective detection of catecholamine compounds, with application to the analysis of epinephrine (EPN) in forensic samples as a proof-of-concept. The method integrates a colorimetric step (Melo Test), based on ferricyanide oxidation in alkaline medium (ammonium buffer), with a two-stage electrochemical protocol employing screen-printed graphite electrodes (SPE-Gr). Three analytical responses are obtained: (i) the oxidation peak of EPN before the colorimetric reaction (O1); (ii) a distinct reddish-orange color following a positive Melo Test for catecholamine structures; and (iii) a new oxidation signal (P1) corresponding to the reaction product. The combined response also enabled discrimination between β-hydroxylated catecholamines and structurally related catecholamines lacking this functionality. The method was optimized using square-wave voltammetry, demonstrating good linearity (6 to 60 μg L-1), low limits of detection (1.5 and 2.3 μg L-1 for O1 and P1, respectively), and high reproducibility (RSD <5% for Ep and Ip). Application to biological matrices (urine, serum, saliva, and vitreous humor) yielded high recoveries, negligible matrix effects, and high selectivity even in the presence of structurally related compounds (18 substances individually and in mixtures). This approach offers a reliable tool for EPN screening in forensic toxicology, with potential extension to other catecholamine analytes.

Indexed as

CatecholaminesElectrochemical TechniquesEpinephrineColorimetryElectrodesGraphiteHumansLimit of DetectionOxidation-ReductionCatecholaminesEpinephrineGraphite

Identifiers

PMID42444331
PMCPMC13425554

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.